Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/79815
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dc.contributor.authorHeise, Niels V.-
dc.contributor.authorStröhl, Dieter-
dc.contributor.authorSchmidt, Theresa-
dc.contributor.authorCsuk, René-
dc.date.accessioned2022-03-30T07:20:09Z-
dc.date.available2022-03-30T07:20:09Z-
dc.date.issued2022-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/81769-
dc.identifier.urihttp://dx.doi.org/10.25673/79815-
dc.description.abstractAmides derived from platanic acid (30-nor-lupane skeleton) were converted in two steps into 21-aza-17,19-ethano-19-nor-urs-20-en-21-ium chlorides. These ursane-skeleton iminium salts are first in their class, and some of them proved as selective inhibitors of the enzyme butyrylcholinesterase while holding no inhibitory activity for acetylcholinesterase.eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc547-
dc.titleStable triterpenoid iminium salts and their activity as inhibitors of butyrylcholinesteraseeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleJournal of molecular structure-
local.bibliographicCitation.volume1249-
local.bibliographicCitation.publishernameElsevier-
local.bibliographicCitation.publisherplaceNew York, NY [u.a.]-
local.bibliographicCitation.doi10.1016/j.molstruc.2021.131646-
local.openaccesstrue-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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